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Renal and prostate stones composition in alkaptonuria: a case report

Authors :
Fleur Wolff
Thierry Roumeguere
Frédéric Cotton
Caroline Koopmansch
Agnieszka Pozdzik
Ibrahim Biaou
Marc Vanden Bossche
Source :
Clinical Nephrology. 84:339-342
Publication Year :
2015
Publisher :
Dustri-Verlgag Dr. Karl Feistle, 2015.

Abstract

Alkaptonuria is a genetic disorder characterized by an accumulation of homogentisic acid due to an enzymatic defect of homogentisate 1,2 dioxygenase. The homogentisic acid is excreted exclusively by both glomerular filtration and tubular secretion leading to the renal parenchyma being exposed to high concentrations of homogentisic acid. The alkaptonuric patients are at higher risk of renal stones (and of prostate stones for males), usually in the later stages of the disease. We describe the case of a 51-year-old man whose renal and prostate stones were analyzed by X-ray diffraction and infrared spectroscopy, respectively. We review the cases of alkaptonuria (AKU) patients reported in the literature for whom the composition of kidney or prostate stones was assessed with physical or chemical techniques. In this paper, we also discuss the advantages and drawbacks of the different methodologies.

Details

ISSN :
03010430
Volume :
84
Database :
OpenAIRE
Journal :
Clinical Nephrology
Accession number :
edsair.doi.dedup.....337cc06255c78258ef4db5c9626779d4
Full Text :
https://doi.org/10.5414/cn108608